Literature DB >> 19456335

Understanding the multifactorial control of growth hormone release by somatotropes: lessons from comparative endocrinology.

Manuel D Gahete1, Mario Durán-Prado, Raúl M Luque, Antonio J Martínez-Fuentes, Ana Quintero, Ester Gutiérrez-Pascual, José Córdoba-Chacón, María M Malagón, Francisco Gracia-Navarro, Justo P Castaño.   

Abstract

Control of postnatal growth is the main, but not the only, role for growth hormone (GH) as this hormone also contributes to regulating metabolism, reproduction, immunity, development, and osmoregulation in different species. Likely owing to this variety of group-specific functions, GH production is differentially regulated across vertebrates, with an apparent evolutionary trend to simplification, especially in the number of stimulatory factors governing substantially GH release. Thus, teleosts exhibit a multifactorial regulation of GH secretion, with a number of factors, from the newly discovered fish GH-releasing hormone (GHRH) to pituitary adenylate cyclase-activating peptide (PACAP) but also gonadotropin-releasing hormone, dopamine, corticotropin-releasing hormone, and somatostatin(s) directly controlling somatotropes. In amphibians and reptiles, GH secretion is primarily stimulated by the major hypothalamic peptides GHRH and PACAP and inhibited by somatostatin(s), while other factors (ghrelin, thyrotropin-releasing hormone) also influence GH release. Finally, in birds and mammals, primary control of GH secretion is exerted by a dual interplay between GHRH and somatostatin. In addition, somatotrope function is modulated by additional hypothalamic and peripheral factors (e.g., ghrelin, leptin, insulin-like growth factor-I), which together enable a balanced integration of feedback signals related to processes in which GH plays a relevant regulatory role, such as metabolic and energy status, reproductive, and immune function. Interestingly, in contrast to the high number of stimulatory factors impinging upon somatotropes, somatostatin(s) stand(s) as the main primary inhibitory regulator(s) for this cell type.

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Year:  2009        PMID: 19456335     DOI: 10.1111/j.1749-6632.2008.03660.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  20 in total

1.  Hindbrain catecholamine neurons modulate the growth hormone but not the feeding response to ghrelin.

Authors:  Alan J Emanuel; Sue Ritter
Journal:  Endocrinology       Date:  2010-05-12       Impact factor: 4.736

2.  Homologous and heterologous in vitro regulation of pituitary receptors for somatostatin, growth hormone (GH)-releasing hormone, and ghrelin in a nonhuman primate (Papio anubis).

Authors:  Jose Córdoba-Chacón; Manuel D Gahete; Justo P Castaño; Rhonda D Kineman; Raul M Luque
Journal:  Endocrinology       Date:  2011-11-22       Impact factor: 4.736

3.  Obestatin plays an opposite role in the regulation of pituitary somatotrope and corticotrope function in female primates and male/female mice.

Authors:  Raúl M Luque; José Córdoba-Chacón; Alejandro Ibáñez-Costa; Iacopo Gesmundo; Cristina Grande; Francisco Gracia-Navarro; Manuel Tena-Sempere; Ezio Ghigo; Manuel D Gahete; Riccarda Granata; Rhonda D Kineman; Justo P Castaño
Journal:  Endocrinology       Date:  2014-01-31       Impact factor: 4.736

4.  Somatostatin is essential for the sexual dimorphism of GH secretion, corticosteroid-binding globulin production, and corticosterone levels in mice.

Authors:  Jessica M Adams; Veronica Otero-Corchon; Geoffrey L Hammond; Johannes D Veldhuis; Nathan Qi; Malcolm J Low
Journal:  Endocrinology       Date:  2014-12-31       Impact factor: 4.736

Review 5.  Does the pituitary somatotrope play a primary role in regulating GH output in metabolic extremes?

Authors:  Raul M Luque; Manuel D Gahete; Jose Cordoba-Chacon; Gwen V Childs; Rhonda D Kineman
Journal:  Ann N Y Acad Sci       Date:  2011-03       Impact factor: 5.691

6.  Evidences for involvement of growth hormone and insulin-like growth factor in ovarian development of starry flounder (Platichthys stellatus).

Authors:  Yongjiang Xu; Bin Wang; Xuezhou Liu; Bao Shi; Kun Zang
Journal:  Fish Physiol Biochem       Date:  2016-11-02       Impact factor: 2.794

7.  A novel reproductive peptide, phoenixin.

Authors:  G L C Yosten; R-M Lyu; A J W Hsueh; O Avsian-Kretchmer; J-K Chang; C W Tullock; S L Dun; N Dun; W K Samson
Journal:  J Neuroendocrinol       Date:  2013-02       Impact factor: 3.627

8.  Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects.

Authors:  Adrian F Daly; Bo Yuan; Frederic Fina; Jean-Hubert Caberg; Giampaolo Trivellin; Liliya Rostomyan; Wouter W de Herder; Luciana A Naves; Daniel Metzger; Thomas Cuny; Wolfgang Rabl; Nalini Shah; Marie-Lise Jaffrain-Rea; Maria Chiara Zatelli; Fabio R Faucz; Emilie Castermans; Isabelle Nanni-Metellus; Maya Lodish; Ammar Muhammad; Leonor Palmeira; Iulia Potorac; Giovanna Mantovani; Sebastian J Neggers; Marc Klein; Anne Barlier; Pengfei Liu; L'Houcine Ouafik; Vincent Bours; James R Lupski; Constantine A Stratakis; Albert Beckers
Journal:  Endocr Relat Cancer       Date:  2016-03-02       Impact factor: 5.678

9.  Molecular cloning and functional characterization of growth hormone-releasing hormone in Mastacembelus armatus.

Authors:  Dongming Zhong; Mingqing Zhang; Xingxing Lan; Shuisheng Li; Hu Shu
Journal:  Fish Physiol Biochem       Date:  2020-10-28       Impact factor: 2.794

10.  Growth hormone and insulin-like growth factor-I alter hippocampal excitatory synaptic transmission in young and old rats.

Authors:  Doris P Molina; Olusegun J Ariwodola; Jeff L Weiner; Judy K Brunso-Bechtold; Michelle M Adams
Journal:  Age (Dordr)       Date:  2012-08-01
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